ClinVar Miner

Submissions for variant NM_001081.4(CUBN):c.10181-31G>A

gnomAD frequency: 0.01027  dbSNP: rs115686202
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001565475 SCV001788828 likely benign not provided 2020-01-16 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001565475 SCV005226961 likely benign not provided criteria provided, single submitter not provided

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